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ORPHA:99771Morphological anomaly
Also called Bifidity of the uvula · Uvular cleft
What it is
Bifid uvula is a fissure type embryopathy affecting the uvula at the back of the soft palate.
Key facts
- Age of onset
- Infancy, Neonatal
- Inheritance
- Multigenic/multifactorial, Not applicable
- Classified as
- Morphological anomaly
Recorded for the broader condition
- Prevalence
- 1-5 / 10 000 (Europe)Cleft palate
Orphanet records these for the broader condition rather than for this specific form. They are a starting point, not a figure for this subtype — subtypes often differ, and some are defined by being rarer than the condition they sit under.
Signs and symptoms
These ranges are how often a sign appears across everyone diagnosed, not a prediction for one person — most people have some of these and not others. Orphanet also records findings that are specifically absent in this disease; those are in the data but not listed here.
Genes
ICD-10 codes
Related health topics
Reached through the ICD-10 categories this disease is filed under, so these describe the broader group rather than this disease specifically.
Cross-references
Orphadata Science: Free access data from Orphanet. © INSERM 1999. Data version 2026-06-23. Available under CC BY 4.0. This is a reference, not medical advice.
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